Electrochemical nanostructuring of (111) oriented GaAs crystals: from porous structures to nanowires

• Elena I. Monaico,
• Eduard V. Monaico,
• Veaceslav V. Ursaki,
• Shashank Honnali,
• Vitalie Postolache,
• Karin Leistner,
• Kornelius Nielsch and
• Ion M. Tiginyanu

Beilstein J. Nanotechnol. 2020, 11, 966–975, doi:10.3762/bjnano.11.81

• these nanowires were tested for field emission, but not for photodetector applications. The nanowires were produced using electrochemical etching under optimized conditions in a mixed H3PO4/HCl electrolyte followed by chemical etching for reducing the diameter down to 150 nm. The authors of the work did

A set of empirical equations describing the observed colours of metal–anodic aluminium oxide–Al nanostructures

• Cristina V. Manzano,
• Jakob J. Schwiedrzik,
• Gerhard Bürki,
• Laszlo Pethö,
• Johann Michler and
• Laetitia Philippe

Beilstein J. Nanotechnol. 2020, 11, 798–806, doi:10.3762/bjnano.11.64

• (yielding to the same porosity), changing only the second anodization time (from 120 to 600 s) to obtain different film thicknesses (from 209 ± 12 nm to 380 ± 15 nm). Focused ion beam (FIB) milling and field-emission scanning electron microscopy (FESEM) imaging were used to accurately determine the

• . After that, the Cr layer was deposited. Characterization of AAO films Morphological characterisation was performed using a field-emission scanning electron microscope (FESEM, Hitachi S-4800) with a 1.5 kV accelerating voltage. The thickness was obtained from sample cross sections fabricated using a

Effect of Ag loading position on the photocatalytic performance of TiO₂ nanocolumn arrays

• Jinghan Xu,
• Yanqi Liu and
• Yan Zhao

Beilstein J. Nanotechnol. 2020, 11, 717–728, doi:10.3762/bjnano.11.59

• structures were observed using a field emission scanning electron microscope (FE-SEM, FEI, Tecnai G2 F30). The elemental composition and valence distribution of the film were measured by X-ray photoelectron spectroscopy (XPS, Thermo Fisher Scientific, ESCALAB 250Xi). The photoluminescence (PL) intensity of

Structural optical and electrical properties of a transparent conductive ITO/Al–Ag/ITO multilayer contact

• Aliyu Kabiru Isiyaku,
• Ahmad Hadi Ali and
• Nafarizal Nayan

Beilstein J. Nanotechnol. 2020, 11, 695–702, doi:10.3762/bjnano.11.57

• IAAI and ITO films was further analyzed by field-emission scanning electron microscopy (FESEM, 5.0 kV, 100000× magnification). Figure 4 shows FESEM images of the as-deposited and annealed IAAI and ITO films. The as-deposited IAAI and ITO films show a smooth and continuous surface with small grains and

• carried out using the Nanoscope Analysis software. All films were scanned over an area of 1 μm × 1 μm. Field-emission scanning electron microscopic analyses The surface morphology of the prepared thin films was further studied using field-emission scanning electron microscopy (FESEM). A FESEM JEOL JSM

Exfoliation in a low boiling point solvent and electrochemical applications of MoO₃

• Matangi Sricharan,
• Bikesh Gupta,
• Sreejesh Moolayadukkam and
• H. S. S. Ramakrishna Matte

Beilstein J. Nanotechnol. 2020, 11, 662–670, doi:10.3762/bjnano.11.52

• preheated oven. The remaining MoO3 powder in the beaker was weighed to determine the concentration. The morphology of MoO3 flakes was characterized using field-emission scanning electron microscopy (FESEM; Tescan Mira3), transmission electron microscopy (TEM; FEI Talos, 200 kV) and atomic force microsopy

Silver-decorated gel-shell nanobeads: physicochemical characterization and evaluation of antibacterial properties

• Marta Bartel,
• Katarzyna Markowska,
• Marcin Strawski,
• Krystyna Wolska and
• Maciej Mazur

Beilstein J. Nanotechnol. 2020, 11, 620–630, doi:10.3762/bjnano.11.49

• ) analysis were performed with a Zeiss Merlin field-emission SEM instrument. Transmission electron microscopy images were collected with a Zeiss Libra 120 EFTEM. Confocal laser scanning microscopy (CLSM) imaging of bacterial biofilms was performed with a Nikon AIR MP microscope equipped with a 60×, NA 1.4

Synthesis and enhanced photocatalytic performance of 0D/2D CuO/tourmaline composite photocatalysts

• Changqiang Yu,
• Min Wen,
• Zhen Tong,
• Shuhua Li,
• Yanhong Yin,
• Xianbin Liu,
• Yesheng Li,
• Tongxiang Liang,
• Ziping Wu and
• Dionysios D. Dionysiou

Beilstein J. Nanotechnol. 2020, 11, 407–416, doi:10.3762/bjnano.11.31

• using step scan mode performed with a DX-2700 diffractometer (Dandong Haoyuan Instrument Co. Ltd., China) with Ni-filtered Cu Kα radiation (λ = 0.1.541 Å), 10–80° 2θ scan. X-ray photoelectron spectra (XPS) were recorded using a K-ALPHA instrument (ThermoFisher Scientific, USA). A MIRA3 field emission

Poly(1-vinylimidazole) polyplexes as novel therapeutic gene carriers for lung cancer therapy

• Gayathri Kandasamy,
• Elena N. Danilovtseva,
• Vadim V. Annenkov and
• Uma Maheswari Krishnan

Beilstein J. Nanotechnol. 2020, 11, 354–369, doi:10.3762/bjnano.11.26

• RNAse-free water and dried overnight. The samples were stained with 1% phosphotungstic acid solution (Merck, Germany) and imaged using high-resolution field-emission transmission electron microscopy (JEM2100F, JEOL, Japan). Differential scanning calorimetry: The melting point of the blank PVI

• . Characterization of the polyplex Electron microscopy: A small drop of the polyplex sample was placed on a conducting carbon tape and air-dried. The sample was then sputter-coated with a thin film of gold. The sample was placed in the sample chamber and imaged at an accelerating voltage of 3 kV using a cold field

• -emission scanning electron microscope (JSM6701F, JEOL, Japan). For transmission electron microscopy, 1 mL of the polyplex was deposited on 400 mesh copper grids (Canemco-Marivac, Canada) and air-dried for 10 min. The excess sample was removed by blotting using a filter paper. The grids were washed using

Simple synthesis of nanosheets of rGO and nitrogenated rGO

• Pallellappa Chithaiah,
• Madhan Mohan Raju,
• Giridhar U. Kulkarni and
• C. N. R. Rao

Beilstein J. Nanotechnol. 2020, 11, 68–75, doi:10.3762/bjnano.11.7

• Mira3 field-emission scanning electron microscope (FESEM) equipped with an energy-dispersive X-ray spectroscopy (EDS). The TEM, HRTEM images and SAED patterns were obtained on a TALOS F200S G2, 200 kV FEG, and a CMOS camera (4k × 4k). The TEM samples were prepared by suspending the samples in ethanol

Synthesis of amorphous and graphitized porous nitrogen-doped carbon spheres as oxygen reduction reaction catalysts

• Maximilian Wassner,
• Markus Eckardt,
• Andreas Reyer,
• Thomas Diemant,
• Michael S. Elsaesser,
• R. Jürgen Behm and
• Nicola Hüsing

Beilstein J. Nanotechnol. 2020, 11, 1–15, doi:10.3762/bjnano.11.1

• Scanning electron microscopy (SEM) images were recorded with a field-emission scanning electron microscope (FE-SEM, Zeiss Ultra Plus) at 10 to 12 keV beam energy. For imaging, the samples were deposited on a conducting carbon film. Energy-dispersive X-ray spectroscopy (EDX) measurements were performed on

Synthesis and acetone sensing properties of ZnFe₂O₄/rGO gas sensors

• Kaidi Wu,
• Yifan Luo,
• Ying Li and
• Chao Zhang

Beilstein J. Nanotechnol. 2019, 10, 2516–2526, doi:10.3762/bjnano.10.242

• ZnFe2O4. In addition, the results of field-emission scanning electron microscopy and (high-resolution) transmission electron microscopy indicated that the synthesized samples had the structure of hollow spheres distributed uniformly onto rGO nanosheets. The diameters of the spheres were determined as

• diffraction (XRD, Bruker D8 Advance) using Cu Kα radiation at room temperature. The 2θ range was 10−80°, and the scanning rate was 5°·min−1. The microscopic morphology and the size of all samples were observed using a field-emission scanning electron microscope equipped with an energy-dispersive spectrometer

• (FESEM, Hitachi S4800). The nanostructure of the products was examined by transmission electron microscopy (TEM, JEM-2100). High-resolution TEM (HRTEM) and energy-dispersive X-ray (EDX) elemental mappings were recorded using a field-emission transmission electron microscope (Tecnai G2 F30 S-TWIN, FEI

Polyvinylpyrrolidone as additive for perovskite solar cells with water and isopropanol as solvents

• Chen Du,
• Shuo Wang,
• Xu Miao,
• Wenhai Sun,
• Yu Zhu,
• Chengyan Wang and
• Ruixin Ma

Beilstein J. Nanotechnol. 2019, 10, 2374–2382, doi:10.3762/bjnano.10.228

• chlorobenzene) at 4500 rpm for 20 s. The above preparation process was carried out under ambient conditions. Finally, the devices were completed by using thermal evaporation and deposited on an Au electrode. Characterization Field-emission scanning electron microscopy (FESEM) images were obtained with a ZEISS

Design and facile synthesis of defect-rich C-MoS₂/rGO nanosheets for enhanced lithium–sulfur battery performance

• Chengxiang Tian,
• Juwei Wu,
• Zheng Ma,
• Bo Li,
• Pengcheng Li,
• Xiaotao Zu and
• Xia Xiang

Beilstein J. Nanotechnol. 2019, 10, 2251–2260, doi:10.3762/bjnano.10.217

• -4, C-MoS2/rGO-6, C-MoS2/rGO-8) with a 3:1 mass ratio was calcined at 155 °C for 12 h in a sealed vessel. Materials characterization The structure and morphology were investigated by field-emission scanning electron microscopy (FE-SEM, INSPECT F50) and transmission electron microscopy (TEM, ZEISS

Ultrathin Ni_1−xCo_xS₂ nanoflakes as high energy density electrode materials for asymmetric supercapacitors

• Xiaoxiang Wang,
• Teng Wang,
• Rusen Zhou,
• Lijuan Fan,
• Shengli Zhang,
• Feng Yu,
• Tuquabo Tesfamichael,
• Liwei Su and
• Hongxia Wang

Beilstein J. Nanotechnol. 2019, 10, 2207–2216, doi:10.3762/bjnano.10.213

• . Notably, the influence of the substrate on the electrochemical performance can be neglected because of its small area of CV curves under the same scan rate (Figure S1, Supporting Information File 1). Material characterization Field-emission scanning electron microscopy (FESEM, JSM-7001F, JEOL) with energy

Mannosylated brush copolymers based on poly(ethylene glycol) and poly(ε-caprolactone) as multivalent lectin-binding nanomaterials

• Stefania Ordanini,
• Wanda Celentano,
• Anna Bernardi and
• Francesco Cellesi

Beilstein J. Nanotechnol. 2019, 10, 2192–2206, doi:10.3762/bjnano.10.212

• acquired with a DeLong America LVEM5 microscope, equipped with a field-emission gun and operating at 5 kV. TEM samples were prepared by dropping 10 µL of sample (10 mg/mL in water) on a copper grid (400 mesh) placed on filter paper. The grid was left to dry overnight for evaporating the solvent

Use of data processing for rapid detection of the prostate-specific antigen biomarker using immunomagnetic sandwich-type sensors

• Camila A. Proença,
• Tayane A. Freitas,
• Thaísa A. Baldo,
• Elsa M. Materón,
• Flávio M. Shimizu,
• Gabriella R. Ferreira,
• Frederico L. F. Soares,
• Ronaldo C. Faria and
• Osvaldo N. Oliveira Jr.

Beilstein J. Nanotechnol. 2019, 10, 2171–2181, doi:10.3762/bjnano.10.210

• spectroscopy (FTIR), field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), and polarization-modulated infrared reflection absorption spectroscopy (PM-IRRAS, Figure S1) is described. The Silhouette coefficients calculated for IDMAP, Sammon’s mapping (SM), principal

Green and scalable synthesis of nanocrystalline kuramite

• Andrea Giaccherini,
• Giuseppe Cucinotta,
• Stefano Martinuzzi,
• Enrico Berretti,
• Werner Oberhauser,
• Alessandro Lavacchi,
• Giovanni Orazio Lepore,
• Giordano Montegrossi,
• Maurizio Romanelli,
• Antonio De Luca,
• Massimo Innocenti,
• Vanni Moggi Cecchi,
• Matteo Mannini,
• Antonella Buccianti and
• Francesco Di Benedetto

Beilstein J. Nanotechnol. 2019, 10, 2073–2083, doi:10.3762/bjnano.10.202

• of nanocrystalline kuramite by means of a simpler, greener and scalable solvothermal synthesis. We exploited a multianalytical characterization approach (X-ray diffraction, extended X-ray absorption fine structure, field emission scanning electron microscopy, Raman spectroscopy and electronic

Facile synthesis of carbon nanotube-supported NiO//Fe₂O₃ for all-solid-state supercapacitors

• Shengming Zhang,
• Xuhui Wang,
• Yan Li,
• Xuemei Mu,
• Yaxiong Zhang,
• Jingwei Du,
• Guo Liu,
• Xiaohui Hua,
• Yingzhuo Sheng,
• Erqing Xie and
• Zhenxing Zhang

Beilstein J. Nanotechnol. 2019, 10, 1923–1932, doi:10.3762/bjnano.10.188

• 12 h. CC-CNT@NiO: The NiO was coated on the CC-CNT by the same process with NiCl2 (0.1 M) aqueous solution instead of FeCl3 (0.1 M). Materials characterization The morphologies and microstructures of the as-prepared samples were characterized by using a field-emission scanning electron microscope (FE

Biocatalytic oligomerization-induced self-assembly of crystalline cellulose oligomers into nanoribbon networks assisted by organic solvents

• Yuuki Hata,
• Yuka Fukaya,
• Toshiki Sawada,
• Masahito Nishiura and
• Takeshi Serizawa

Beilstein J. Nanotechnol. 2019, 10, 1778–1788, doi:10.3762/bjnano.10.173

• with osmium. The fracture surface was observed by a field-emission scanning electron microscope (JSM-7500F, JEOL) at an accelerating voltage of 5 kV. Analysis of the secondary structure of CDP The secondary structure of CDP was analyzed by CD spectroscopy. CDP was dissolved in a 8 mM phosphate buffer

Development of a new hybrid approach combining AFM and SEM for the nanoparticle dimensional metrology

• Loïc Crouzier,
• Alexandra Delvallée,
• Sébastien Ducourtieux,
• Laurent Devoille,
• Guillaume Noircler,
• Christian Ulysse,
• Olivier Taché,
• Elodie Barruet,
• Christophe Tromas and
• Nicolas Feltin

Beilstein J. Nanotechnol. 2019, 10, 1523–1536, doi:10.3762/bjnano.10.150

• silicon substrates through the spin-coating method detailed in [11]. This method yields well-dispersed nanoparticles on the substrate while maximizing the number of isolated NPs preventing agglomeration of the NPs. NP SEM images have been recorded using a Zeiss ULTRA-Plus field-emission (FE) microscope

• information about the NP height, whereas the uncertainty associated with the AFM measurement of the NP maximum point is close to 1.5 nm [1]. Conversely, the lateral dimensions measured by AFM are impacted by tip/NP convolution, whereas latest-generation scanning electron microscopes equipped with field

• -emission guns can reach a resolution of 1 nm in the XY-plane. Consequently, we propose in this paper the development of a hybrid metrology that allows for the measurement of the characteristic dimensions of a nano-object in 3D, by combining the measurements performed with AFM and SEM. The concept of hybrid

Hierarchically structured 3D carbon nanotube electrodes for electrocatalytic applications

• Pei Wang,
• Katarzyna Kulp and
• Michael Bron

Beilstein J. Nanotechnol. 2019, 10, 1475–1487, doi:10.3762/bjnano.10.146

• discovery in 1991 [1] due to their high electrical conductivity, large surface area, good chemical stability, high mechanical strength and high aspect ratio and are considered as promising materials for diverse applications such as field emission displays, energy storage devices, sensors, and so on [2][3][4

Direct observation of oxygen-vacancy formation and structural changes in Bi₂WO₆ nanoflakes induced by electron irradiation

• Hong-long Shi,
• Bin Zou,
• Zi-an Li,
• Min-ting Luo and
• Wen-zhong Wang

Beilstein J. Nanotechnol. 2019, 10, 1434–1442, doi:10.3762/bjnano.10.141

• = 1.5406 Å). Morphological analyses were carried out on a field-emission scanning electron microscope (SEM, Hitachi S-4800) equipped with an energy-dispersive X-ray spectroscopy (EDX) detector operating at 10 kV and 10 μA. Selected-area electron diffraction (SAED) and high-resolution transmission electron

Selective gas detection using Mn₃O₄/WO₃ composites as a sensing layer

• Yongjiao Sun,
• Zhichao Yu,
• Wenda Wang,
• Pengwei Li,
• Gang Li,
• Wendong Zhang,
• Lin Chen,
• Serge Zhuivkov and
• Jie Hu

Beilstein J. Nanotechnol. 2019, 10, 1423–1433, doi:10.3762/bjnano.10.140

• yellow, pure WO3 and Mn3O4/WO3 composites. Apparatus and instruments X-ray power diffraction (XRD) data was collected on a Rigaku D/Max-2550 V diffractometer with Cu Kα1 radiation (= 1.54178 Å) at 25 mA and 35 kV. Field emission scanning electron microscopy (FE-SEM) images were recorded on a JEM-7100F

The effect of magneto-crystalline anisotropy on the properties of hard and soft magnetic ferrite nanoparticles

• Hajar Jalili,
• Bagher Aslibeiki,
• Ali Ghotbi Varzaneh and
• Volodymyr A. Chernenko

Beilstein J. Nanotechnol. 2019, 10, 1348–1359, doi:10.3762/bjnano.10.133

• order to determine the particle size distribution and morphology of the samples, field-emission scanning electron microscopy (FE-SEM) was carried out. Figure 3 shows FE-SEM images of all the samples. The images reveal that particles are in the nanometer range and roughly spherical in shape. The

• transform infrared (FTIR) spectra of the samples were obtained in the range of 400–4000 cm−1 by pressing the powders in KBr pellets. The morphology and elemental chemical composition of the samples were investigated using a Tescan Mira 3 field-emission scanning electron microscope (FE-SEM) equipped with an

Fabrication of phase masks from amorphous carbon thin films for electron-beam shaping

• Lukas Grünewald,
• Dagmar Gerthsen and
• Simon Hettler

Beilstein J. Nanotechnol. 2019, 10, 1290–1302, doi:10.3762/bjnano.10.128

• analysis of a PM before placing it in the condenser system. We used a TITAN 80-300 (Thermo Fisher Scientific) operated at 300 kV (λ = 1.97 pm) equipped with a field-emission gun. Nearly parallel illumination of the PM was achieved by working in the low-magnification mode (LM mode). In this setup, the